JPS5978301A - Synthetic resin lens - Google Patents

Synthetic resin lens

Info

Publication number
JPS5978301A
JPS5978301A JP57189616A JP18961682A JPS5978301A JP S5978301 A JPS5978301 A JP S5978301A JP 57189616 A JP57189616 A JP 57189616A JP 18961682 A JP18961682 A JP 18961682A JP S5978301 A JPS5978301 A JP S5978301A
Authority
JP
Japan
Prior art keywords
lens
absorber
contg
formula
group
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP57189616A
Other languages
Japanese (ja)
Other versions
JPH047481B2 (en
Inventor
Satoshi Kubota
久保田 聰
Takao Mogami
最上 隆夫
Junji Kawashima
川嶋 淳史
Yoshio Sano
良夫 佐野
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Seiko Epson Corp
Suwa Seikosha KK
Original Assignee
Seiko Epson Corp
Suwa Seikosha KK
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Seiko Epson Corp, Suwa Seikosha KK filed Critical Seiko Epson Corp
Priority to JP57189616A priority Critical patent/JPS5978301A/en
Publication of JPS5978301A publication Critical patent/JPS5978301A/en
Publication of JPH047481B2 publication Critical patent/JPH047481B2/ja
Granted legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B1/00Optical elements characterised by the material of which they are made; Optical coatings for optical elements
    • G02B1/04Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29DPRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
    • B29D11/00Producing optical elements, e.g. lenses or prisms
    • B29D11/0073Optical laminates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29DPRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
    • B29D11/00Producing optical elements, e.g. lenses or prisms
    • B29D11/00865Applying coatings; tinting; colouring

Landscapes

  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Ophthalmology & Optometry (AREA)
  • Mechanical Engineering (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Surface Treatment Of Optical Elements (AREA)
  • Moulds For Moulding Plastics Or The Like (AREA)

Abstract

PURPOSE:To obtain a lens superior in abrasion resistance hy radically polymerizing a mixture of contg. a styrene type monomer, a specified cross-linkable monomer, and a UV absorber to obtain a lens base, and coating its surface with its surface with a hard coat layer contg. a specified silane compd. and a reflection preventive layer made of an inorganic substance in this order. CONSTITUTION:The lens base 1 is prepared by radically polymerizing a mixture contg. 9-80pts.wt. sytrene type monomer represented by formula I (X is halogen except F, or H; Y is halogen except F; and R is H or CH3; (m) is 1-5; and (n) is 0-3), 20-80pts.wt. cross-linkable monomer represented by formula II, and 0.01-1.0pt.wt. UV absorber, such as benzotriazole. On both surface of the less base 1 are formed a hard coat layer 2 contg. as an essential component a compd. represented by formula III (R' is an org. group having an epoxy group or gamma-methacryloxypropyl; R<2> is H or 1-4C org. group; Z is halogen except F, or alkoxy; and k+l is 0-2), and further, a polyfunctional epoxy compd. and a UV absorber having been hardened, and a reflection preventing layer 3 having SiO2 or ZrO2 or the like vapor deposited.

Description

【発明の詳細な説明】 本発明は、合成樹)信としては比較的屈折率の高い樹脂
製レンズの表面に、紫外線吸収剤勿含む育成のハードコ
ート層【設け、さらにその上に、無磯物力・らなん単層
または多ノーの反則防止Jm h設けた合成樹l后製レ
ンズに関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides, on the surface of a synthetic resin lens, which has a relatively high refractive index, a grown hard coat layer containing an ultraviolet absorber, and furthermore, a hard coat layer containing an ultraviolet absorber. This invention relates to a lens made of synthetic resin with a single layer or multi-layer anti-fouling material.

合FM、梱崩製レンズは、焦域ガラスレンズに較べ軽い
、耐衝撃性が高い、加工性が艮いなど柚々の長)f+紮
有している。しかし、反面、一般の樹脂製レンズμ、屈
折率がガラスに比べて低り、また、強度的に中心厚r厚
く保つ必要もあり、全体として厚くならざるゲ得な71
”つた。だが、近年的屈折率の樹脂製レンズの開発も行
なわれており、市販もされている。一般式LI〕で示さ
れろ1棟以上の単量体79刀1ら80重量部と、一般式
[11]で示される1棟以上の単重体i20刀1ら80
康瀘部勿ラジカル重合させfこ@成樹脂製レンズもその
代表的なものである。しかし、該合Fli、憫血製レン
ズは、その構造中に炭素−ハロゲン結片が’HD、5B
υ11 m付近の光で容易にps離する為、耐候性が悪
いという欠点がある。また、原料のメチレフ11本も耐
候性が悪い上に、)i躬防止コーティング加工でさらに
大きなダメージヶ受けてしまう。ゆえに、耐候性向上の
為、紫外線吸収剤7人八で裔1いるものの、表面付近で
の効果1よ博く、最外部での具素のps +ii!によ
る黄変Vユ避けられない。
FM and Bakugo lenses have many advantages such as being lighter, having higher impact resistance, and being easier to work with than focal range glass lenses. However, on the other hand, the refractive index of general resin lenses μ is lower than that of glass, and it is also necessary to keep the center thickness r thick for strength reasons, so the overall thickness cannot be increased.
However, in recent years, resin lenses with a modern refractive index have been developed and are commercially available.As shown by the general formula LI], one or more monomers 79 to 1 to 80 parts by weight, , one or more single bodies i20 sword 1 and 80 represented by the general formula [11]
Lenses made of synthetic resin made by radical polymerization are also typical. However, the lens made of Fli, 5B, has carbon-halogen fragments in its structure.
Since it is easily separated by ps with light around υ11 m, it has the disadvantage of poor weather resistance. In addition, the 11 pieces of Metilef used as raw materials have poor weather resistance, and are subject to even greater damage due to the anti-corrosion coating. Therefore, in order to improve weather resistance, although there are 7 UV absorbers and 8 UV absorbers and 1 descendant, the effect near the surface is greater than 1, and the effect of the material at the outermost layer is PS +II! Yellowing caused by V-yu is unavoidable.

また、憎脂襄レンズの別な欠点として、耐擦傷性が劣る
点があけられる、この為、レンズ表面にハードコード層
r)M丁必女があ6゜−万、眼鏡レンズの場せ、表1反
荊の低減に対する決望が強く前記合成樹1信義レンズQ
CおいてVよ、酸化ケイ素ケ主体としたハードコート層
ケ設け、その上に、無機柳刃)らなる単層またに多鳩の
反則防止層ケ施丁方法が用いられている。このガ法μ、
寸分艮い反荊防止効未rj:得られるが、耐擦傷性1J
1まだ十分といえるものは得られていない。また、東1
威1勿の厚いハードコート層で施している為、耐1剪隼
件がコート前に較べ、極度に悪くなるという欠点もある
In addition, another disadvantage of the anti-grease lens is that it has poor scratch resistance.For this reason, there is a hard code layer on the lens surface. Table 1 Synthetic tree 1 Xinyi lens Q with strong determination to reduce rumination
In C and V, a hard coat layer mainly composed of silicon oxide is provided, and a single layer or multiple anti-fouling layers made of inorganic willow blades are applied thereon. This method μ,
Significant rumination prevention effect: achieved, but scratch resistance 1J
1.I have not yet obtained anything that can be said to be sufficient. Also, East 1
Since it is coated with a very thick hard coat layer, it also has the disadvantage that the shear resistance is extremely poor compared to before coating.

本発明は、刀1〃)る欠点を除去したもので、その目的
は、耐候性、耐擦傷性、耐衝撃性に優れ、反則防止効果
が大きく、軽くて薄い会成悄脂製しンズr提供する事に
ある。
The present invention eliminates the disadvantages of sword 1).The purpose of the present invention is to make lightweight and thin Kaisei resin lenses that are excellent in weather resistance, scratch resistance, and impact resistance, have a large foul prevention effect, and are lightweight and thin. It is about providing.

すなわち、本発明は、(A)−収式口〕で示される1株
以上の単量体79カーら80重量部と、一般式〔■〕で
示される1橿以上の単量体12071・ら80重量部お
よび紫外線吸収剤tα01〃1ら1.0重量都営むモノ
マーの混合液ケラジカル重合させた合成樹脂レンズ基材
表面に、 0−0=CH,〔If ] 1 (式中、Xiフッ素を除くハロゲンまたVよ水素、Yr
J、フッ素會除くハロゲ7、Rrl:水素またrユメチ
ル基、mは1から5、nl工0かも60企戚を表わ丁) (B)  一般式Llll〕で示される有愼シラン化合
物の1橿ま几は2橿以上の混合物τ主成分とし、こjL
に多1能注エポキシ化合物と紫外線吸収剤勿6ミ加して
硬化した1から30μmのノ・−トコ−) )d k施
し、 1 1 J          L[l) R’)、 −51−24−k−1 (式中、H4μエポキシ端′jf:1丁ゐ有機基またV
ユT−メタクロリロキシグロピルM、R”は水素またμ
炭素数1〃)ら4の有機基、2はフッ素に除くノ・ロゲ
ンまたはアルコキシ基、k十lは口から2の整叔を表わ
す) <a)  さらに、前記ノ・−トコーH−上に、無礪′
吻〃1らなゐ単層ま1こは多ノーの膜厚0.5 p m
以Fの反則防止層紫膜けた事r肪畝とする合成1ソ4噛
映レンズに関するものである。
That is, the present invention comprises 80 parts by weight of one or more monomers 79 and 12071 and 80 parts by weight of one or more monomers represented by the general formula [■] A mixed solution of monomers containing 80 parts by weight and ultraviolet absorber tα01〃1 and 1.0 parts by weight Toei was applied to the surface of the chemically radically polymerized synthetic resin lens base material. Excluding halogen, V, hydrogen, Yr
(B) One of the silane compounds represented by the general formula Lllll] A mixture of two or more substances τ is the main component, and this jL
A multifunctional epoxy compound and an ultraviolet absorber were added and cured to a thickness of 1 to 30 μm. k-1 (in the formula, H4μ epoxy end 'jf: 1-2 organic group or V
UT-methacryloxyglopyr M, R” is hydrogen or μ
an organic group having 1 to 4 carbon atoms; 2 is a fluorine or alkoxy group excluding fluorine; , no loss′
The thickness of the monolayer is 0.5 pm.
The following relates to a synthetic 1-4-shape lens in which the anti-fouling layer has a violet film with ridges and ridges.

本発明の基本的な膜構成μ、吊1図のノInりであり、
8成側脂製Vンズ1上に、紫外線吸収剤ヶ含む有償のハ
ードコート・謔2と、無懺′lfIからなる単)−また
Vニレ)−の反則防止111j 5が設けられていゐ。
The basic membrane configuration μ of the present invention is the same as in Figure 1,
On the plastic V-lens 1, there is provided a paid hard coat 2 containing an ultraviolet absorber, and a non-fouling prevention 111j 5 consisting of an unstainable V-lens.

会曾側月旨製レンズ1の原孝り防貝LILL■jお工び
紫外線吸収剤の混合比は、特許請求の範囲で述べた割合
にエリ、眼礎レンズに請求され/S時性r満足させるこ
とができる。単量体LIFの組成比が9繊量都未満の場
合には、レンズの耐衝阜強就が低下し、80iL′jj
k部ケ越えると耐熱性1.玉摺加工性が著しく低下する
。単量体[1]の組成比が20重量部未満の場合には、
単量体LIEの場合とは逆で、耐熱性、玉摺加工性が低
下し、80車欺部r越すと耐1Av−性が低下し、レン
ズに要求される特性?満足できない、 合成樹脂製レンズ1に用いる紫外線吸収剤としては、ベ
ンゾトリアゾール系、ベンゾフェノン系、シアノアクリ
レート系、サリチレート系があめ。
The mixing ratio of the ultraviolet absorber used in the lens 1 made by Tsukiji on the Eisen side is the ratio stated in the claims, and the ratio claimed in the fundus lens is /S chronological r can be satisfied. When the composition ratio of monomer LIF is less than 9 fibers, the impact resistance of the lens decreases, and the
Heat resistance above part k is 1. Tamazuri workability is significantly reduced. When the composition ratio of monomer [1] is less than 20 parts by weight,
Contrary to the case of monomer LIE, the heat resistance and abrasive workability decrease, and when the temperature exceeds 80 degrees, the 1Av-resistance decreases, which characteristics are required for lenses? Unsatisfactory UV absorbers used in the synthetic resin lens 1 include benzotriazole, benzophenone, cyanoacrylate, and salicylate.

有f幾のハードコートj曽2μ、合6父樹11旨レンズ
の表面硬度r筒めろと同時に、紫外線吸収剤によってレ
ンズ基材を光から保映し、また、無機物からなる反射防
止嗜とレンズとのそ層性2同上させる事にエリ、レンズ
の耐擦傷性、耐候性ケ総合的に向上させている。
The surface hardness of the lens is 2μ, 2μ, 11μ, and at the same time, the lens base material is protected from light by the ultraviolet absorber, and the anti-reflection lens is made of inorganic material. In addition, the scratch resistance and weather resistance of the lens are improved overall.

該有機ハードコート曽20組1戎としては、一般式[1
[1) (式中、R’はエポキシ&、tMする有機基またはメタ
クロイルオキシエチル4 、R2は水素または炭素数1
刀)ら4の有機基、Zμフッ素kW<ハロケンまたはア
ルコキシ基、k+1は0刀)ら2の蟹数7表わす)で示
されろ有機シラン化合物の1個またrI2I2上の混合
物?主成分とし、これに多官能性エボキン化合物と紫外
線吸収剤會添別している。
As the organic hard coat 20 sets 1 coat, the general formula [1
[1] (In the formula, R' is an epoxy &, tM organic group or methacroyloxyethyl 4, R2 is hydrogen or a carbon number of 1
One of the organosilane compounds or a mixture on rI2I2? The main component is a polyfunctional Evoquin compound and a UV absorber.

該多官能性エポキシ化合物としては、ポリオレフィン系
エポキシ樹月旨、7クロペンタジエンオキシドあるいは
へキザヒドロフタル酸とエピクロルヒドリンから得られ
るポリグリシジルエステルなどの月旨環式エポキシ樹)
[旨、ビスフェノールAやカテコール、レゾルノノール
ナトの多1曲フェノールあるいμ(ボリンエチレ〕/グ
リコール、(ポリンプロピレングリコール、ネオペンチ
ルグリコール、グリセリン、ヘキザメチレングリコール
、トリメチロールプロパン、ペンタエリスリトール、ジ
グリセロール、ソルビトール とエピクロルヒドリン刀1らイ得られるポリグリシジル
エーテルなどがあげられる。
Examples of the polyfunctional epoxy compound include polyolefin-based epoxy resins, cyclic epoxy resins such as 7-clopentadiene oxide, or polyglycidyl esters obtained from hexahydrophthalic acid and epichlorohydrin.
[Items include bisphenol A, catechol, resolnonol, phenol or μ (borine ethylene) / glycol, (polypropylene glycol, neopentyl glycol, glycerin, hexamethylene glycol, trimethylolpropane, pentaerythritol, Examples include polyglycidyl ethers obtained from glycerol, sorbitol and epichlorohydrin.

有機ハードコート層に重加される紫外線吸収剤としては
、ベンゾトリアゾール系、ベンゾフェノン系、シアノア
クリレート系、サリチレート系がある。
Examples of ultraviolet absorbers added to the organic hard coat layer include benzotriazole-based, benzophenone-based, cyanoacrylate-based, and salicylate-based.

バートコ−) 1m 2の膜厚は、1μm未満では、十
分な耐擦傷性が得られず、30μm’f超えると十分な
表面硝朋が得られない。
If the film thickness is less than 1 μm, sufficient scratch resistance will not be obtained, and if it exceeds 30 μm'f, sufficient surface glass will not be obtained.

反則防止層3汀、単層または矛盾の無機物の層で構成さ
れ、用いられる無機物としては、Sin,。
Foul prevention layer 3 is composed of a single layer or a layer of contradictory inorganic materials, and the inorganic material used is Sin.

Zr02 、 Ti04 、 Tat03 、 Ylo
g 、 ’#b103 、 Ag2O3等の金属酸化物
、Si3N.等の金属窒化物、MrF,等の金属フッ化
物、Or, W, Ta等の金属がある。無機物の層r
@成樹脂レしズ上に厚くコートすると、レン;(の耐衝
撃性が著しく低下する。不発明においては、無機物の膜
厚に0.5μm以Fにおさえることで、レンズの耐#卓
性r株付している。
Zr02, Ti04, Tat03, Ylo
g, '#b103, metal oxides such as Ag2O3, Si3N. There are metal nitrides such as, metal fluorides such as MrF, and metals such as Or, W, and Ta. inorganic layer
@ If a thick coating is applied to a synthetic resin lens, the impact resistance of the lens will be significantly reduced. In the invention, by keeping the inorganic film thickness to 0.5 μm or more, the impact resistance of the lens will be significantly reduced. It has r shares.

以下、実施例に基づいて本発明2評しく線間する。Hereinafter, two aspects of the present invention will be discussed based on examples.

実施例 スチレン50重量部、2,2−ビスし3.5−ジプロモ
−4 − ( 2−メタクリロイルオキシェトキシフフ
ェニル〕グロバン4a3重量部、t−ブチルパーオキシ
ピバレート1.5JijtftL  2 − (2’−
ヒドロキシ−5′−メチルフェニルラベンゾトリアゾー
ル0.2重ii部の共重合体製の合Fj又樹脂製しンズ
上に、紫外線吸収剤7合む有機ハードコートj!# k
施し、さらにその上に、sio,+ 、 Zr02 上
すなる5 101の反射防止11!llk設けた。有機
ハードコート層は、テトラメトキシシラン2 9 0i
jdi、γーグリシドオキシプロピルトリメトキシシラ
ン8。
Example 50 parts by weight of styrene, 3 parts by weight of 2,2-bis-3,5-dipromo-4-(2-methacryloyloxyethoxyphenyl)globan 4a, 1.5 parts by weight of t-butylperoxypivalate −
An organic hard coat made of a copolymer of 0.2 parts of hydroxy-5'-methylphenylrabenzotriazole and 7 parts of an ultraviolet absorber on the resin film! #k
Alms, and on top of that, sio, +, Zr02 top 5 101 anti-reflection 11! llk was established. The organic hard coat layer is made of tetramethoxysilane 290i
jdi, γ-glycidoxypropyltrimethoxysilane 8.

TL菫部お工び1,6−ヘキサフシオールジグリシジル
エーテル104重j#を都のイ昆合1勿7メチルエチル
ケトン233i量部と酢酸100厘Jt@の混合溶媒液
とし、0.05規定塩酸188本量部で加水分解した浴
液に紫外線吸収i’?11として7−(2’−ヒドロキ
シ−5′−メチルフェニルノペンゾトリアゾール1.5
車量部お工び硬化〕甥媒として塩化第一スズ0.5車量
部に加えて調整し、ディッピングに工り塗布し、150
℃で2時間熱硬化し1こ。ハード−1−)の膜厚は、5
5μmである。また、前記反別防止層1ユ、真空蒸層法
にエリ施し、その膜厚は0・3μmである。
TL Sumirebe's 1,6-hexafushiol diglycidyl ether 104 heavy j# was made into a mixed solvent solution of 233 parts of methyl ethyl ketone and 100 Jt of acetic acid, and 0.05N hydrochloric acid. 188 parts of hydrolyzed bath liquid contains ultraviolet absorption i'? 11 as 7-(2'-hydroxy-5'-methylphenylnopenzotriazole 1.5
[Currently hardening] Adjust by adding 0.5 parts of stannous chloride as a solvent, apply to dipping, and apply to 150 parts.
Heat cured at ℃ for 2 hours. The film thickness of Hard-1-) is 5
It is 5 μm. In addition, one layer of the anti-separation layer was formed using a vacuum evaporation method, and its film thickness was 0.3 μm.

爽、9イ11ンリ−2 実施例−1における育成ハードコート内の紫外線吸収剤
72.2’−ジヒドロキシ−4−メトキシベンゾフェノ
ンに変えた以外μ実施例−1に同じ。
Sou, 9-11-2 Same as Example-1 except that the ultraviolet absorber 72 in the growing hard coat in Example-1 was changed to 2'-dihydroxy-4-methoxybenzophenone.

実施例−5 実施例−1における有穢ハードコート内の紫外m 吸収
剤にエチル−2−ンアへづ 3/−ジフエ・ニルアクリ
レートに変えた以外tユ実施し1l−1に同じ。
Example 5 The same procedure as 1l-1 was carried out except that the UV absorber in Example 1 was changed to ethyl-2-ahenyl 3/-diphenylacrylate.

実施例 実施例−1における有歳ハートコート内の紫外1d牧収
剤χP−tθrtプチルフェニルザIJチL/−)に笈
えた以夕tμ芙施11−1に同じ。
Example Same as tμ 11-1, which was introduced in the ultraviolet 1d harvesting agent χP-tθrtbutylphenylza IJchiL/-) in the aged heart coat in Example-1.

参照ψリ−1 実施91J’−1における有償ハードコート内の紫外線
吸収剤r除い友以外に実〃出β用−1に同じ。
Reference ψ Lee-1 Same as the production β-1 except for the ultraviolet absorber r in the paid hard coat in Example 91J'-1.

参照列−2 実施列−1における有へ涜71−トコ−)+四の代わり
に、AltOB、 SiO’l 、 ZrO2刀)らl
る無→のノ1−ドコートを真空蒸7#法により施した。
Reference column-2 Instead of the 71-toko-) + 4 in the implementation column-1, AltOB, SiO'l, ZrO2 sword) et al.
A blank node coat was applied by the vacuum evaporation 7# method.

そり膜厚は、2.2μmである。The warpage film thickness is 2.2 μm.

耐候性試験eこは、キセノ/ンングフェードメーターτ
用い、評価は、フェードメーターに1000時間かけた
麦の黄変嫂?肉視で利足した。
Weather resistance test
Used and evaluated is wheat yellowing after 1000 hours on a fade meter? I was able to see it with the naked eye.

耐俤鵠注評価は、gUυ00スチールウールに1盈荷嵐
rかけ10佳諷した結果【、−ガラス’7Aアクリル樹
脂でE′として、10段階でt′F価しlこ。
The durability rating was obtained by applying 1 coat to 100% of gUυ00 steel wool. -Glass'7A acrylic resin was graded as E' and t'F was graded on a scale of 10.

耐衝撃性は、FDA規q□fq V+−往栢するか否ρ
1で判定した。
Impact resistance is determined by FDA standards q□fq V+-
It was judged as 1.

#fIlIIi結果r表−1に示す。#fIlIIi Results are shown in Table-1.

表−1 以上のように、本発明は、耐候性、耐僚揚性に劣る高屈
折率合成#4脂製レンズに、紫外線吸収剤ケきむ有囁ノ
・−ドコート曽と無賊物f)>らなる反則防止層ケ施す
楽に工って、優れた劇侯性、耐際傷性ケ与え、さらに、
耐衝撃性の向上、反則率の低減も併せて行なうことので
きる画期的なものである。
Table 1 As described above, the present invention has the advantage of adding an ultraviolet absorber to a high refractive index synthetic #4 resin lens that has poor weather resistance and flight resistance. >The anti-fouling layer is easy to apply, provides excellent durability and scratch resistance, and
This is an epoch-making product that also improves impact resistance and reduces the foul rate.

【図面の簡単な説明】[Brief explanation of drawings]

第1図μ、本発明の基本的な膜構成図である。 1は合成団脂襄レンズ、2は紫外線吸収剤會含む有懺ハ
ードコート曽、3は反則防止層である。 以上
FIG. 1 μ is a basic membrane configuration diagram of the present invention. 1 is a synthetic resin lens, 2 is a coated hard coat containing an ultraviolet absorber, and 3 is a fouling prevention layer. that's all

Claims (1)

【特許請求の範囲】 (A)  一般式[1]で示されろ1棟以上のJ41量
体t9〃1ら80車量部と、一般式[ll]で示される
1棟以上の単瀘体22oから80嵐量部および紫外線吸
収剤τ0. (117)kら1. [11重量部含むモ
ノマーの混合液tラジカル本台させたせ楓樹脂レンズ基
材表面に、 (式中、Xはフッ素τ朔<〕・ロゲンまたは水系、Yl
l’mフッ系才味〈ハロゲン、Rは水系またはメチル基
、01ぼ1刀1ら5、nはO刀1ら6の整奴7表わ丁う (E)  一般式[111Jで示さt″Lる育成/ラン
化合物の1棟または2棟以上の混合物ケ玉成分とし、こ
れに多官能エポキシ化付物と裕外線吸収剤孕冷カII 
t。 て硬化し1こ1で)ら30μmのハードコート層ケ施し
、 (式中、R′はエポキシ基才何する/に儂番またμγ−
メタクリロキシプロピル基 Hlは水素または炭素数1
〃・ら4の肩戦基、Zμフッ素ケ除くハロゲンまたV:
Iアルコキシ基、k+lは0刀)ら2の整数?表わす) (C)  さらに、前記ハードJ−ト層上に、無4戊両
刀)らなる単層または多増の膜厚05μm以[の反躬防
止盾r設けた$ケ特徴とする合成4ffl Ili製レ
ンズ。
[Scope of Claims] (A) One or more J4 monomers t9 1 to 80 parts by mass represented by the general formula [1] and one or more monomers represented by the general formula [ll] 22° to 80° part and ultraviolet absorber τ0. (117) k et al. 1. [A mixture of monomers containing 11 parts by weight of radicals is applied to the surface of the maple resin lens base material, (wherein,
l'm Fluorine-based talent〈Halogen, R is water-based or methyl group, 01 is 1 to 1 to 5, n is Oto to 1 to 6, 7 expressions (E) General formula [111J indicates t ``L growth/A mixture of one or two or more orchid compounds is used as an ingredient, and this is combined with a polyfunctional epoxidized adjunct and a Yugai ray absorber.
t. (In the formula, R' is an epoxy base material.
Methacryloxypropyl group Hl is hydrogen or has 1 carbon number
〃・Ra4 shoulder base, Zμ fluorine, halogen or V:
I alkoxy group, k + l is an integer of 0) and 2? (C) Further, on the hard layer, a single layer or multiple anti-repulsion shields with a thickness of 05 μm or more are provided. made lens.
JP57189616A 1982-10-28 1982-10-28 Synthetic resin lens Granted JPS5978301A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57189616A JPS5978301A (en) 1982-10-28 1982-10-28 Synthetic resin lens

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57189616A JPS5978301A (en) 1982-10-28 1982-10-28 Synthetic resin lens

Publications (2)

Publication Number Publication Date
JPS5978301A true JPS5978301A (en) 1984-05-07
JPH047481B2 JPH047481B2 (en) 1992-02-12

Family

ID=16244277

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57189616A Granted JPS5978301A (en) 1982-10-28 1982-10-28 Synthetic resin lens

Country Status (1)

Country Link
JP (1) JPS5978301A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60262833A (en) * 1984-06-11 1985-12-26 Tokuyama Soda Co Ltd Coated synthetic resin material
JPS61108636A (en) * 1984-11-02 1986-05-27 Toray Ind Inc Production of antireflection composite material
JPS61259664A (en) * 1985-05-15 1986-11-17 日本板硝子株式会社 Artificial crystal lens and its production
US4732454A (en) * 1985-04-22 1988-03-22 Toray Industries, Inc. Light-transmissible plate shielding electromagnetic waves
JPS6428617A (en) * 1987-07-24 1989-01-31 Fujitsu Ltd Projection type liquid crystal display device
WO2002096628A3 (en) * 2001-05-29 2003-02-27 Essilor Int Method for forming on-site a coated optical article
JP2008285305A (en) * 2007-05-21 2008-11-27 Shin Meiwa Ind Co Ltd Garbage collection truck
CN108789980A (en) * 2017-04-26 2018-11-13 句容大为网络科技有限公司 A kind of panchromatic resin lens moulding process of novel UV photocurings

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60262833A (en) * 1984-06-11 1985-12-26 Tokuyama Soda Co Ltd Coated synthetic resin material
JPH0129376B2 (en) * 1984-06-11 1989-06-09 Tokuyama Soda Kk
JPS61108636A (en) * 1984-11-02 1986-05-27 Toray Ind Inc Production of antireflection composite material
US4732454A (en) * 1985-04-22 1988-03-22 Toray Industries, Inc. Light-transmissible plate shielding electromagnetic waves
JPS61259664A (en) * 1985-05-15 1986-11-17 日本板硝子株式会社 Artificial crystal lens and its production
JPH0472548B2 (en) * 1985-05-15 1992-11-18 Nippon Ita Garasu Kk
JPS6428617A (en) * 1987-07-24 1989-01-31 Fujitsu Ltd Projection type liquid crystal display device
WO2002096628A3 (en) * 2001-05-29 2003-02-27 Essilor Int Method for forming on-site a coated optical article
US6890458B2 (en) 2001-05-29 2005-05-10 Essilor International Compagnie General D'optique Method for forming on-site a coated optical article
JP2008285305A (en) * 2007-05-21 2008-11-27 Shin Meiwa Ind Co Ltd Garbage collection truck
CN108789980A (en) * 2017-04-26 2018-11-13 句容大为网络科技有限公司 A kind of panchromatic resin lens moulding process of novel UV photocurings

Also Published As

Publication number Publication date
JPH047481B2 (en) 1992-02-12

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